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rs587777459

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777459(C;T)
Make rs587777459(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position31815005
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs587777459
ebirs587777459
HLIrs587777459
Exacrs587777459
Varsomers587777459
Maprs587777459
PheGenIrs587777459
hapmaprs587777459
1000 genomesrs587777459
hgdprs587777459
ensemblrs587777459
gopubmedrs587777459
geneviewrs587777459
scholarrs587777459
googlers587777459
pharmgkbrs587777459
gwascentralrs587777459
openSNPrs587777459
23andMers587777459
23andMe allrs587777459
SNP Nexus

SNPshotrs587777459
SNPdbers587777459
MSV3drs587777459
GWAS Ctlgrs587777459
Max Magnitude0
ClinVar
Risk rs587777459(G,T;G,T)
Alt rs587777459(G,T;G,T)
Reference rs587777459(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32210991C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128401.2,